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An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host

Egg parasitoids have evolved adaptations to exploit host-associated cues, especially oviposition-induced plant volatiles and odors of gravid females, when foraging for hosts. The entire host selection process is critical for successful parasitism and relevant in defining host specificity of parasito...

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Autores principales: Bertoldi, Valeria, Rondoni, Gabriele, Brodeur, Jacques, Conti, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6621923/
https://www.ncbi.nlm.nih.gov/pubmed/31333475
http://dx.doi.org/10.3389/fphys.2019.00746
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author Bertoldi, Valeria
Rondoni, Gabriele
Brodeur, Jacques
Conti, Eric
author_facet Bertoldi, Valeria
Rondoni, Gabriele
Brodeur, Jacques
Conti, Eric
author_sort Bertoldi, Valeria
collection PubMed
description Egg parasitoids have evolved adaptations to exploit host-associated cues, especially oviposition-induced plant volatiles and odors of gravid females, when foraging for hosts. The entire host selection process is critical for successful parasitism and relevant in defining host specificity of parasitoids. We hypothesized that naïve egg parasitoid females reared on their coevolved host are able to exploit cues related to the coevolved host but not those from a novel host. We used the egg parasitoid Trissolcus japonicus, its coevolved host Halyomorpha halys, and the non-coevolved host Podisus maculiventris to evaluate this hypothesis. H. halys, a polyphagous pest native from Eastern Asia, has invaded North America and Europe, resulting in serious damage to crops. T. japonicus is the most effective egg parasitoid of H. halys in its native area and thus considered a major candidate for biological control. This parasitoid was detected in North America and Europe as a result of accidental introductions. Laboratory host range of T. japonicus includes P. maculiventris, an American predatory stink bug used as a biological control agent of several pests. Using T. japonicus reared on its natural host H. halys, we tested in a Y-tube olfactometer the responses of naïve parasitoid females to volatiles from tomato plants with a deposited egg mass and feeding punctures of either H. halys or P. maculiventris. Additionally, using two different olfactometer set-ups, we tested T. japonicus responses to volatiles emitted by eggs and mature males and females of H. halys or P. maculiventris. Tomato plants subjected to oviposition and feeding by H. halys were preferred by the wasp compared to clean plants, suggesting a possible activation of an indirect defense mechanism. Furthermore, T. japonicus females were attracted by cues from gravid females and mature males of H. halys but not from eggs. By contrast, naïve parasitoid females never responded to cues associated with P. maculiventris, although this non-target host is suitable for complete parasitoid development. Such lack of responses might reduce the probability of T. japonicus locating and parasitizing P. maculiventris under field conditions. Our experimental approach properly simulates the parasitoid host-location process and could be combined with the required host specificity tests for risk assessment in biological control programs.
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spelling pubmed-66219232019-07-22 An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host Bertoldi, Valeria Rondoni, Gabriele Brodeur, Jacques Conti, Eric Front Physiol Physiology Egg parasitoids have evolved adaptations to exploit host-associated cues, especially oviposition-induced plant volatiles and odors of gravid females, when foraging for hosts. The entire host selection process is critical for successful parasitism and relevant in defining host specificity of parasitoids. We hypothesized that naïve egg parasitoid females reared on their coevolved host are able to exploit cues related to the coevolved host but not those from a novel host. We used the egg parasitoid Trissolcus japonicus, its coevolved host Halyomorpha halys, and the non-coevolved host Podisus maculiventris to evaluate this hypothesis. H. halys, a polyphagous pest native from Eastern Asia, has invaded North America and Europe, resulting in serious damage to crops. T. japonicus is the most effective egg parasitoid of H. halys in its native area and thus considered a major candidate for biological control. This parasitoid was detected in North America and Europe as a result of accidental introductions. Laboratory host range of T. japonicus includes P. maculiventris, an American predatory stink bug used as a biological control agent of several pests. Using T. japonicus reared on its natural host H. halys, we tested in a Y-tube olfactometer the responses of naïve parasitoid females to volatiles from tomato plants with a deposited egg mass and feeding punctures of either H. halys or P. maculiventris. Additionally, using two different olfactometer set-ups, we tested T. japonicus responses to volatiles emitted by eggs and mature males and females of H. halys or P. maculiventris. Tomato plants subjected to oviposition and feeding by H. halys were preferred by the wasp compared to clean plants, suggesting a possible activation of an indirect defense mechanism. Furthermore, T. japonicus females were attracted by cues from gravid females and mature males of H. halys but not from eggs. By contrast, naïve parasitoid females never responded to cues associated with P. maculiventris, although this non-target host is suitable for complete parasitoid development. Such lack of responses might reduce the probability of T. japonicus locating and parasitizing P. maculiventris under field conditions. Our experimental approach properly simulates the parasitoid host-location process and could be combined with the required host specificity tests for risk assessment in biological control programs. Frontiers Media S.A. 2019-07-04 /pmc/articles/PMC6621923/ /pubmed/31333475 http://dx.doi.org/10.3389/fphys.2019.00746 Text en Copyright © 2019 Bertoldi, Rondoni, Brodeur and Conti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Bertoldi, Valeria
Rondoni, Gabriele
Brodeur, Jacques
Conti, Eric
An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host
title An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host
title_full An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host
title_fullStr An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host
title_full_unstemmed An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host
title_short An Egg Parasitoid Efficiently Exploits Cues From a Coevolved Host But Not Those From a Novel Host
title_sort egg parasitoid efficiently exploits cues from a coevolved host but not those from a novel host
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6621923/
https://www.ncbi.nlm.nih.gov/pubmed/31333475
http://dx.doi.org/10.3389/fphys.2019.00746
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